K-number	K923231
Device name	CARDIO-PAK BASIC PUMP PACK
Applicant	Cardio-Med-Associates, Inc.
Product code	DWE
Device class	Class II
Decision date	Jul 9, 1993
Decision	Unknown
Regulation	870.4390

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View the full FDA submission: accessdata.fda.gov

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CARDIO-PAK BASIC PUMP PACK

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